Sodium Hydroxide → HCID 59608157, compound

HRID 2384030Notes

Reaction equation

HRID 2384030 reaction equation
C([O:3][C:4](=[O:33])[C@H:5]([CH3:32])[CH2:6][C@H:7]([NH:21][C:22]([C:24]1[S:25][C:26]([C:29](=[O:31])[NH2:30])=[CH:27][CH:28]=1)=[O:23])[CH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:11][CH:10]=1)C.[OH-].[Na+]>C(O)C>[C:12]1([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:11]=[CH:10][C:9]([CH2:8][C@@H:7]([NH:21][C:22]([C:24]2[S:25][C:26]([C:29](=[O:31])[NH2:30])=[CH:27][CH:28]=2)=[O:23])[CH2:6][C@@H:5]([CH3:32])[C:4]([OH:33])=[O:3])=[CH:14][CH:13]=1

Participants

4

Conditions

Temperature
50 °C

Procedure

Next, to a solution of (2R,4S)-5-biphenyl-4-yl-4-[(5-carbamoyl-thiophene-2-carbonyl)-amino]-2-methyl-pentanoic acid ethyl ester (115 mg, 0.248 mmol) in ethanol (8 mL) is added aqueous 1M NaOH (0.866 mL, 0.866 mmol) and the mixture is stirred at 50° C. for 3.5 hours. The ethanol is removed under reduced pressure and water is added to the residue. The resulting solution is acidified with aqueous 1M HCl and the resulting precipitate is filtered and washed with water. The solid is purified by preparative HPLC using 50% MeCN/water to elute the product. The appropriate fractions are lyophilized to give (2R,4S)-5-biphenyl-4-yl-4-[(5-carbamoyl-thiophene-2-carbonyl)-amino]-2-methyl-pentanoic acid. MS 437.2 (M+1); 1H-NMR (400 MHz, DMSO-d6); δ ppm 1.09 (d, J=7.20 Hz, 3H), 1.57 (m, 1H), 1.88 (m, 1H), 2.46 (m, 1H), 2.84 (m, 2H), 4.18 (m, 1H), 7.28 (d, J=8.21 Hz, 1H), 7.33 (t, 1H), 7.44 (t, 1H), 7.57 (d, J=8.21 Hz, 2H), 7.64 (d, J=7.33, 2H), 7.69 (m, 2H), 8.06 (s, 1H), 8.38 (d, J=8.59 Hz, 1H), 12.07 (s, broad, 1H).

Workup

  1. customThe ethanol is removed under reduced pressure and water
  2. additionis added to the residue
  3. filtrationthe resulting precipitate is filtered
  4. washwashed with water
  5. customThe solid is purified by preparative HPLC
  6. washto elute the product

Sources & evidence

ORD record
ord-b87db64d041146b3909b3f643a2af91a
Source dataset
uspto-grants-2012_09
Patent number
US08263629B2

Reaction notes

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