Hydrochloric Acid → HCID 86625732, compound

HRID 2110238Notes

Reaction equation

HRID 2110238 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-df73010d580244078c4ee8a356e21354
Source dataset
uspto-grants-2009_04
Patent number
US07517874B2

Reaction notes

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