1-Hydroxybenzotriazole → HCID 178466807, compound

HRID 1096901Notes

Reaction equation

HRID 1096901 reaction equation
C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl.[CH2:23]([O:25][C:26]1[CH:27]=[C:28]([CH:32]=[C:33]([O:42][CH2:43][CH3:44])[C:34]=1[C:35]1[CH:36]=[N:37][C:38]([F:41])=[CH:39][CH:40]=1)[C:29]([OH:31])=O)[CH3:24].Cl.[NH:46]1[C:50]([C:51]2[CH:52]=[C:53]3[C:63](=[CH:64][CH:65]=2)[O:62][C:56]2([CH2:61][CH2:60][NH:59][CH2:58][CH2:57]2)[CH2:55][C:54]3=[O:66])=[N:49][N:48]=[N:47]1>O.CN(C=O)C.CCN(CC)CC>[CH2:43]([O:42][C:33]1[CH:32]=[C:28]([C:29]([N:59]2[CH2:60][CH2:61][C:56]3([CH2:55][C:54](=[O:66])[C:53]4[C:63](=[CH:64][CH:65]=[C:51]([C:50]5[NH:49][N:48]=[N:47][N:46]=5)[CH:52]=4)[O:62]3)[CH2:57][CH2:58]2)=[O:31])[CH:27]=[C:26]([O:25][CH2:23][CH3:24])[C:34]=1[C:35]1[CH:36]=[N:37][C:38]([F:41])=[CH:39][CH:40]=1)[CH3:44]

Participants

8

Procedure

Et3N (200 μL), HOBT (110 mg) and WSC hydrochloride (138 mg) were added to a DMF (4 mL) solution of 3,5-diethoxy-4-(6-fluoropyridin-3-yl)benzoic acid (186 mg) and 6-(tetrazol-5-yl)spiro[chroman-2,4′-piperidin]-4-one hydrochloride (231 mg), and stirred overnight at room temperature. Water was added to the reaction liquid, the formed solid was taken out through filtration, and the solid was washed with water and ether. The solid was dried under reduced pressure to obtain the title compound. 1H-NMR (400 MHz, DMSO-d6) δ: 8.42 (1H, d, J=4.0 Hz), 8.24 (1H, dd, J=8.0, 4.0 Hz), 8.13 (1H, s), 7.89 (1H, dt, J=8.0, 4.0 Hz), 7.32 (1H, d, J=8.0 Hz), 7.18 (1H, dd, J=8.0, 4.0 Hz), 6.75 (2H, s), 4.32-4.18 (1H, m), 4.08 (4H, q, J=8.0 Hz), 3.64-3.20 (3H, m), 2.98 (2H, s), 2.10-1.75 (4H, m), 1.17 (6H, t, J=8.0 Hz). MS [M+H]+=573.

Workup

  1. filtrationthe formed solid was taken out through filtration
  2. washthe solid was washed with water and ether
  3. customThe solid was dried under reduced pressure

Sources & evidence

ORD record
ord-9a51cea638a64a51b6c75b6e197ec9f4
Source dataset
uspto-grants-2012_03
Patent number
US08138197B2

Reaction notes

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