Hydrochloric Acid → HCID 86625732, compound

HRID 1971128Notes

Reaction equation

HRID 1971128 reaction equation
[F:1][C:2]([CH3:17])([CH3:16])[CH:3]([NH:8]C(=O)OC(C)(C)C)[C:4]([NH:6][CH3:7])=[O:5].[ClH:18].C(OCC)C>ClCCl>[ClH:18].[NH2:8][CH:3]([C:2]([F:1])([CH3:17])[CH3:16])[C:4]([NH:6][CH3:7])=[O:5]

Participants

5

Procedure

Intermediate 66B (306 mg, 1.23 mmol) was dissolved in dichloromethane (5 mL) and was treated with 2M hydrochloric acid solution in diethyl ether (6.18 mL, 12.4 mmol). The resulting mixture was stirred for 2 hour then was concentrated under reduced pressure. The oily residue was dried overnight in a 40° C. vacuum oven to provide intermediate 66C as an off-white solid in quantitative yield. 1H-NMR (400 MHz, (CD3)2SO) δ: 1.38 (d, 3H), 1.43 (d, 3H), 2.67 (d, 3H), 3.97 (d, 1H), 8.51 (broad s, 3H), 8.76 (q, 1H).

Workup

  1. concentrationthen was concentrated under reduced pressure
  2. customThe oily residue was dried overnight in a 40° C. vacuum oven

Sources & evidence

ORD record
ord-fc270f0fd54f4339a04da55c5895d6a7
Source dataset
uspto-grants-2013_04
Patent number
US08431565B2

Reaction notes

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